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DOID:0112239 - X-linked lissencephaly 1
Disease Ontology Definition:A lissencephaly characterized by classic lissencephaly and intellectual disability in males that has_material_basis_in mutation in DCX on chromosome Xq23.
Synonyms: XLIS1, lissencephaly type 1 due to doublecortin gene mutation,
Xenbase Genes :
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee